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논문 기본 정보

자료유형
학술저널
저자정보
Zhen, Ao Xuan (Jeju National University School of Medicine and Jeju Research Center for Natural Medicine) Piao, Mei Jing (Jeju National University School of Medicine and Jeju Research Center for Natural Medicine) Hyun, Yu Jae (Jeju National University School of Medicine and Jeju Research Center for Natural Medicine) Kang, Kyoung Ah (Jeju National University School of Medicine and Jeju Research Center for Natural Medicine) Ryu, Yea Seong (Jeju National University School of Medicine and Jeju Research Center for Natural Medicine) Cho, Suk Ju (Jeju National University School of Medicine and Jeju Research Center for Natural Medicine) Kang, Hee Kyoung (Jeju National University School of Medicine and Jeju Research Center for Natural Medicine) Koh, Young Sang (Jeju National University School of Medicine and Jeju Research Center for Natural Medicine) Ahn, Mee Jung (Laboratory of Veterinary Anatomy, College of Veterinary Medicine, Jeju National University) Kim, Tae Hoon (Department of Food Science and Biotechnology, Daegu University) Hyun, Jin Won (Jeju National University School of Medicine and Jeju Research Center for Natural Medicine)
저널정보
한국응용약물학회 Biomolecules & Therapeutics(구 응용약물학회지) Biomolecules & therapeutics 제27권 제4호
발행연도
2019.1
수록면
395 - 403 (9page)

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Purpurogallin, a natural phenol obtained from oak nutgalls, has been shown to possess antioxidant, anticancer, and anti-inflammatory effects. Recently, in addition to ultraviolet B (UVB) radiation that induces cell apoptosis via oxidative stress, particulate matter 2.5 ($PM_{2.5}$) was shown to trigger excessive production of reactive oxygen species. In this study, we observed that UVB radiation and $PM_{2.5}$ severely damaged human HaCaT keratinocytes, disrupting cellular DNA, lipids, and proteins and causing mitochondrial depolarization. Purpurogallin protected HaCaT cells from apoptosis induced by UVB radiation and/or $PM_{2.5}$. Furthermore, purpurogallin effectively modulates the pro-apoptotic and anti-apoptotic proteins under UVB irradiation via caspase signaling pathways. Additionally, purpurogallin reduced apoptosis via MAPK signaling pathways, as demonstrated using MAPK-p38, ERK, and JNK inhibitors. These results indicate that purpurogallin possesses antioxidant effects and protects cells from damage and apoptosis induced by UVB radiation and $PM_{2.5}$.

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